Home GUDID 20195860020719
E3D-A Interbody System
Primary DI 20195860020719
Brand E3D-A Interbody System
Company Evolution Spine LLC
Model 111H-S0814
Catalog number 111H-S0814
Device description HAnano STATIC Ti ALIF 32 X 24mm 8deg 14mm (P 11mm)
Published 2024-02-13
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true
Product Codes# Code, Name table Code Name MAX Intervertebral fusion device with bone graft, lumbar OVD Intervertebral fusion device with integrated fixation, lumbar PHM Intervertebral fusion device with bone graft, thoracic
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic 2 OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar Orthopedic 2 PHM Intervertebral Fusion Device With Bone Graft, Thoracic Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 20195860020719 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 20195860020719 20195860020719
GMDN Terms# Term, Definition table Term Definition Metallic spinal interbody fusion cage A device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.
Device Sizes# Type, Value, Unit table Type Value Unit Angle 8 degree Depth 24 Millimeter Height 14 Millimeter Width 32 Millimeter
Sterilization Methods# Method table Method Radiation Sterilization
Regulatory Flags# DUNS number 116940934 Device count 1 Lot or batch true Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published M719GLL100QC0 3DP Lumbar Interbody System Genesys Orthopedics Systems LLC MAX 2026-07-14 M719GLL101QC0 3DP Lumbar Interbody System Genesys Orthopedics Systems LLC MAX 2026-07-14 M719GLL106QC0 3DP Lumbar Interbody System Genesys Orthopedics Systems LLC MAX 2026-07-14 M719GLL107QC0 3DP Lumbar Interbody System Genesys Orthopedics Systems LLC MAX 2026-07-14 08800043913099 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913105 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913112 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913129 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913136 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913143 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913150 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913167 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913174 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913181 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913198 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913204 N/A TDM Co., Ltd. MAX 2026-06-10 08800043913211 N/A TDM Co., Ltd. MAX 2026-06-10 08800043917288 N/A TDM Co., Ltd. MAX 2026-06-10 08800043917295 N/A TDM Co., Ltd. MAX 2026-06-10 08800043917301 N/A TDM Co., Ltd. MAX 2026-06-10 08800043917318 N/A TDM Co., Ltd. MAX 2026-06-10 08800043917325 N/A TDM Co., Ltd. MAX 2026-06-10 08800043917332 N/A TDM Co., Ltd. MAX 2026-06-10 08800043917349 N/A TDM Co., Ltd. MAX 2026-06-10 08800043967177 N/A TDM Co., Ltd. MAX 2026-06-10 08800043967184 N/A TDM Co., Ltd. MAX 2026-06-10 08800043967191 N/A TDM Co., Ltd. MAX 2026-06-10 08800043967207 N/A TDM Co., Ltd. MAX 2026-06-10 08800043967214 N/A TDM Co., Ltd. MAX 2026-06-10 08800043967221 N/A TDM Co., Ltd. MAX 2026-06-10